Actively Recruiting

Phase Not Applicable
Age: 18Years +
FEMALE
NCT06885788

Uterine Round Ligament Preservation Vs Resection in Laparoscopic Inguinal Hernia Repair in Women:A Multicenter,Stratified Randomized Controlled Trial

Led by Nanchong Central Hospital · Updated on 2025-03-25

466

Participants Needed

1

Research Sites

127 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study aims to compare the clinical effects of uterine round ligament preservation versus resection in laparoscopic inguinal hernia repair in women.The primary outcomes included Time required for patient surgery.The secondary outcomes included Inguinal hernia recurrence,quality of life assessment,Indicators of postoperative recovery,, et al.

CONDITIONS

Official Title

Uterine Round Ligament Preservation Vs Resection in Laparoscopic Inguinal Hernia Repair in Women:A Multicenter,Stratified Randomized Controlled Trial

Who Can Participate

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Female patients over 18 years of age without a childbearing requirement
  • Diagnosed with unilateral inguinal hernia
  • Agreed to participate and signed informed consent form
Not Eligible

You will not qualify if you...

  • Severe heart, liver, kidney, or other serious diseases
  • Pregnant or lactating women
  • Patients with surgical contraindications

AI-Screening

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Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Nanchong Central Hospital

Nanchong, Sichuan, China, 637000

Actively Recruiting

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

8

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